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HRID 477500作成日:2026年10月26日

Cyclopropanecarbonyl chloride → HCID 14819887、化合物

https://huagongshe.com/reaction/477500

反応式

関与物質

役割名称HCID仕込み量
反応物Cyclopropanecarbonyl chlorideHCID 77637—
反応物5-MethylisoxazoleHCID 79833—
反応物Lithium diisopropylamideHCID 2724682—
反応物LithiumHCID 3028194—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
溶媒HexaneHCID 8058—
生成物HCID 14819887HCID 1481988729.9%

反応条件

温度-78 °C

反応手順

n-Buyllithium (19.44 ml, 52.5 mmole of a 2.7 M solution in hexane) was added at -15° C. to a solution of diisopropylalmine (5.31g, 52.5 mmole) in 80 ml of dry THF. After 10 min the cooling bath was lowered to -70° C. and 5-methylisoxazole (4.15 g, 50 mmoles) was added to the lithium diidopropylalmine (LDA) solution followed in 30 min by the dropwise addition of cyclopropanecarboxylic acid chloride (5.33 g, 50 mmoles) in 15 ml of THF. The reaction mixture was then stirred at -78° C. for 30 min and at ambient temperature for 2 h. The solvents were evaporated and the residue was partitioned between ether, 30 ml of water and 13 ml of 4 N NaOH. The aqueous layer was separated, acidified with 6 N HCl and extracted with two portions of ether. The extracts were dried and evaporated to a slushy solid that was cchromatographed on 100 g of silica gel using methylene chloride-Skellysolve B (95:5). The appropriate fractions were combined and concentrated to yield 2.26 g of the title compound as a yellow-tinted solid, mp 62°-63.5° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04888357
出典データセットuspto-grants-1989_12
ORD IDord-09ac9aefe91141aa93355a3918e89440
出典メモuspto-grants-1989_12